Oxyplicacetin

CHF 140.00
In stock
BVT-0031-M0011 mgCHF 140.00
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Product Details
Synonyms 3′-Hydroxyplicacetin; Cytosaminomycin E
Product Type Chemical
Properties
Formula

C25H35N5O8

MW 533.6
CAS 100108-92-7
Source/Host Chemicals Isolated from Streptomyces sp.
Purity Chemicals ≥98% (NMR)
Appearance White solid.
Solubility Soluble in DMSO or water.
Identity Determined by 1H-NMR.
Declaration Manufactured by BioViotica.
InChi Key UYEYXSOGZWDEFY-LJEPMGMESA-N
Smiles CC1O[C@H](C[C@@H](O)[C@@H]1O[C@H]1OC(C)[C@H]([C@H](O)C1O)N(C)C)N1C=CC(NC(=O)C2=CC=C(N)C=C2)=NC1=O
Shipping and Handling
Shipping AMBIENT
Short Term Storage +4°C
Long Term Storage +4°C
Handling Advice Protect from light when in solution.
Use/Stability Stable for at least 1 year after receipt when stored at +4°C.
Documents
MSDS Download PDF
Product Specification Sheet
Datasheet Download PDF
  • Nucleoside antibiotic (amicetin group).
  • Anticoccidial agent.
  • Shows broad antibacterial activity.
Product References
  1. Studies on metabolites produced by Streptomyces ramulosus Tue-34. II. The structural elucidation of oxyplicacetin, a new amicetin: Y. Chen, et al.; Kangshengsu 10, 285 (1985) (Chinese)
  2. Cytosaminomycins, new anticoccidial agents produced by Streptomyces sp. KO-8119. I. Taxonomy, production, isolation and physico-chemical and biological properties: K. Haneda, et al.; J. Antibiot. 47, 774 (1994)
  3. Cytosaminomycins, new anticoccidial agents produced by Streptomyces sp. KO-8119. II. Structure elucidation of cytosaminomycins A, B, C and D: K. Shiomi, et al.; J. Antibiot. 47, 782 (1994)
  4. Characterization of the amicetin biosynthesis gene cluster from Streptomyces vinaceusdrappus NRRL 2363 implicates two alternative strategies for amide bond formation: G. Zhang, et al.; Appl. Environ. Microbiol. 78, 2393 (2012)
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